Oxalyl chloride → 3-Hydroxy-4-oxo-3-[(trimethylazaniumyl)methyl]pentanoate
Reaction equation
Cl.[C:2]([C:5]([CH2:12][C:13](=[O:15])[O-:14])([CH2:7][N+:8]([CH3:11])([CH3:10])[CH3:9])[OH:6])(=[O:4])[CH3:3].C(Cl)(=O)C(Cl)=O>>[C:2]([C:5]([CH2:12][C:13](=[O:14])[O-:15])([CH2:7][N+:8]([CH3:9])([CH3:11])[CH3:10])[OH:6])(=[O:4])[CH3:3]Participants
3
Procedure
To acetyl carnitine hydrochloride (1.2 g; 0.005 moles) oxalyl chloride (2.5 ml; 0.029 moles) was added and the resulting mixture was kept under stirring at room temperature for 2 hours. The mixture was then dried under vacuum, the residue was washed three times with anhydrous ethyl ether, thus obtaining the acid chloride of acetyl carnitine which was used as such in the next step.
Workup
- customThe mixture was then dried under vacuum
- washthe residue was washed three times with anhydrous ethyl ether
Sources & evidence
- ORD record
- ord-1cc4b4e3d2c44144bbcf3082faeec084
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343947
Reaction notes
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